Canonical Allele Identifier: CA348161412

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121736029T>G (hg19) ; chr2:g.120978453T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978453T>G , CM000664.2:g.120978453T>G	GRCh38
NC_000002.11:g.121736029T>G , CM000664.1:g.121736029T>G	GRCh37
NC_000002.10:g.121452499T>G	NCBI36
NG_009030.1:g.186163T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1337T>G MANE Select	ENSP00000354586.5:p.Ile446Ser
ENST00000452319.6:c.1388T>G	ENSP00000390436.1:p.Ile463Ser
ENST00000314490.15:c.401T>G	ENSP00000312694.12:p.Ile134Ser
ENST00000341310.10:c.*436T>G	ENSP00000344473.6:n.*436T>G
ENST00000361492.8:c.1388T>G	ENSP00000354586.4:p.Ile463Ser
ENST00000435313.6:n.1362T>G
ENST00000437950.5:c.*487T>G	ENSP00000415773.1:n.*487T>G
ENST00000438299.5:c.*487T>G	ENSP00000400593.1:n.*487T>G
ENST00000445186.5:c.*487T>G	ENSP00000397488.1:n.*487T>G
ENST00000452319.5:c.1388T>G	ENSP00000390436.1:p.Ile463Ser
ENST00000452692.5:c.*436T>G	ENSP00000403715.1:n.*436T>G
NM_005270.4:c.1388T>G	NP_005261.2:p.Ile463Ser
XM_006712422.1:c.1337T>G	XP_006712485.1:p.Ile446Ser
XM_011510969.1:c.1370T>G	XP_011509271.1:p.Ile457Ser
XM_011510970.1:c.1247T>G	XP_011509272.1:p.Ile416Ser
XM_011510971.1:c.1193T>G	XP_011509273.1:p.Ile398Ser
XM_011510972.1:c.1193T>G	XP_011509274.1:p.Ile398Ser
XM_011510973.1:c.1013T>G	XP_011509275.1:p.Ile338Ser
XM_011510974.1:c.962T>G	XP_011509276.1:p.Ile321Ser
XM_006712422.3:c.1337T>G	XP_006712485.1:p.Ile446Ser
XM_011510969.2:c.1640T>G	XP_011509271.2:p.Ile547Ser
XM_011510970.2:c.1247T>G	XP_011509272.1:p.Ile416Ser
XM_011510971.2:c.1193T>G	XP_011509273.1:p.Ile398Ser
XM_011510972.2:c.1289T>G	XP_011509274.2:p.Ile430Ser
XM_011510973.2:c.1013T>G	XP_011509275.1:p.Ile338Ser
XM_011510974.2:c.962T>G	XP_011509276.1:p.Ile321Ser
XM_017003818.1:c.1589T>G	XP_016859307.1:p.Ile530Ser
XM_024452794.1:c.1388T>G	XP_024308562.1:p.Ile463Ser
XM_024452795.1:c.1388T>G	XP_024308563.1:p.Ile463Ser
NM_001371271.1:c.1388T>G	NP_001358200.1:p.Ile463Ser
NM_001374353.1:c.1337T>G MANE Select	NP_001361282.1:p.Ile446Ser
NM_001374354.1:c.962T>G	NP_001361283.1:p.Ile321Ser
NM_005270.5:c.1388T>G	NP_005261.2:p.Ile463Ser